text.skipToContent text.skipToNavigation

Maximum quantity allowed is 999

Please select the quantity

CAS RN: 527-61-7 | Product Number: D2234

2,6-Dimethyl-1,4-benzoquinone


Purity: >98.0%(GC)
Synonyms:
  • 2,6-Dimethyl-2,5-cyclohexadiene-1,4-dione
  • 2,6-Dimethyl-p-quinone
  • m-Xyloquinone
  • DMBQ
Product Documents:
1G
$105.00
1   1   ≥60 
5G
$312.00
5   1   26  
25G
$1,246.00
1   1   6  

* Items in stock locally ship in 1-2 business days. Items from Japan stock are able to ship from a US warehouse within 2 weeks. Please contact TCI for lead times on items not in stock. Excludes regulated items and items that ship on ice.
* To send your quote request for bulk quantities, please click on the "Request Quote" button. Please note that we cannot offer bulk quantities for some products.
*TCI frequently reviews storage conditions to optimize them. Please note that the latest information on the storage temperature for the products is described on our website.


Product Number D2234
Purity / Analysis Method >98.0%(GC)
Molecular Formula / Molecular Weight C__8H__8O__2 = 136.15 
Physical State (20 deg.C) Solid
Storage Temperature Room Temperature (Recommended in a cool and dark place, <15°C)
CAS RN 527-61-7
Reaxys Registry Number 2041345
PubChem Substance ID 87568672
SDBS (AIST Spectral DB) 22842
MDL Number

MFCD00001605

Specifications
Appearance Light yellow to Brown to Dark green powder to crystal
Purity(GC) min. 98.0 %
Melting point 71.0 to 74.0 °C
Properties (reference)
Melting Point 73 °C
GHS
Related Laws:
RTECS# DK4825000
Transport Information:
HS Number 2914.69.9000
Application
Mukaiyama Oxidation-Reduction Condensation

Experimental procedure: under argon atmosphere, a secondary alcohol (0.66 mmol) and 1 (0.66 mmol) in 1,2-dichloroethane (0.6 mL) are stirred for 7.0 h at 100 °C. To a mixture of benzoic acid (0.60 mmol) and 2,6-dimethyl-1,4-benzoquinone (0.6 mmol) is added the above reaction solution. The reaction is stirred for 1.0 h at room temperature and is quenched by adding water after completion of the reaction. The aqueous layer is extracted with dichloromethane. The combined organic layer is washed with brine and dried over anhydrous sodium sulfate. After filtration and evaporation, the resulting residue is purified by preparative TLC to afford the corresponding esters.

References


PubMed Literature


TCIMAIL
Product Documents (Note: Some products will not have analytical charts available.)
Safety Data Sheet (SDS)
Please select Language.

The requested SDS is not available.

Please Contact Us for more information.

Specifications
C of A & Other Certificates
Please enter Lot Number Incorrect Lot Number. Please input only the 4-5 alphanumeric characters before the hyphen.

The product with the lot number searched for has been discontinued and no related documentation is available.

Sample C of A
This is a sample C of A and may not represent a recently manufactured lot of the product.

A sample C of A for this product is not available at this time.

Analytical Charts
Please enter Lot Number Incorrect Lot Number. Please input only the 4-5 alphanumeric characters before the hyphen.

The requested analytical chart is not available. Sorry for the inconvenience.

The product with the lot number searched for has been discontinued and no related documentation is available.

Other Documents

Session Status
Your session will timeout in 10 minutes. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page. minute. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page.

Your session has timed out. You will be redirected to the HOME page.